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首页> 外文期刊>Journal of health science. >Intracisternal Administration of p-n-Octy I phenol into Neonatal Rats Causes Hyperactivity Concomitantly with the Terminal Deoxynucleotidyl Transferase-Mediated dUTP Nick End-Labelling (TUNEL)-Positive Cells in the Mesencephalon where Immunoreactivit
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Intracisternal Administration of p-n-Octy I phenol into Neonatal Rats Causes Hyperactivity Concomitantly with the Terminal Deoxynucleotidyl Transferase-Mediated dUTP Nick End-Labelling (TUNEL)-Positive Cells in the Mesencephalon where Immunoreactivit

机译:对新生大鼠的脑内颅内施用p-n-Octy I苯酚会导致中枢神经元中末端脱氧核苷酸转移酶介导的dUTP尼克末端标记(TUNEL)阳性细胞活动亢进。

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It is unknown which endocrine disruptors exert their effects on neuronal functions, particularly leading to behavioral alterations. To address this, we examined the effects of p-n-octylphenol, an endocrine disruptor, on rat behavior and cellular responses. Single intracisternal administration of p-n-octylphenol (87 nmol) into 5-day-old male Wistar rats caused significant hyperactivity at 4-5 weeks of age. The treated rats were about 1.5-fold more active in the nocturnal phase after administration of p-n-octylphenol than control rats. Immunoljistochemical analyses revealed that p-n-octylphenol Abolished immunoreactivity for tyrosine hydroxylase in the midbrain of 8 week-old rats, where terminal deoxynucleotidyl transferase-mediated dUTP nick end-labelling (TUNEL)-positive cells were also seen. Thus, this is the first demonstration that p-n-octylphenol certainly affected the developing brain, resulting in hyperactivity in the rat, most likely due to degeneration of mesencephalic tyrosine hydroxylase.
机译:尚不清楚哪种内分泌干扰物会影响神经元功能,特别是导致行为改变。为了解决这个问题,我们研究了内分泌干扰物对-正辛基苯酚对大鼠行为和细胞反应的影响。对5日龄的雄性Wistar大鼠单次脑膜内施用对正辛基苯酚(87 nmol)在4-5周龄时引起明显的过度活跃。在施用对-正辛基苯酚后,治疗的大鼠在夜间阶段的活性比对照大鼠高约1.5倍。免疫化学分析表明,对-正辛基苯酚在8周龄大鼠的中脑中对酪氨酸羟化酶的免疫反应性降低,在那里还观察到末端脱氧核苷酸转移酶介导的dUTP缺口末端标记(TUNEL)阳性细胞。因此,这是第一个证明对-正辛基苯酚确实会影响发育中的大脑,从而导致大鼠活动亢进的证据,这很可能是由于中脑酪氨酸羟化酶的变性所致。

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